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Structure of 1184298-27-8
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This boronate reagent features a strategically positioned bromine atom adjacent to a methyl group on the phenyl ring, enabling selective cross-coupling reactions. The electron-deficient aryl boron moiety facilitates efficient palladium-catalyzed transformations under standard conditions. Its bench-stable nature simplifies handling and integration into complex synthetic sequences.
(3-Bromo-2-methylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. The ortho-bromine and methyl groups provide predictable regiochemistry and enhanced stability during storage and handling. Its compatibility with diverse reaction partners and ease of purification make it well-suited for applications in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: